Department of Pharmacology & Toxicology, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.
J Pharm Pharmacol. 2012 Nov;64(11):1659-66. doi: 10.1111/j.2042-7158.2012.01548.x. Epub 2012 May 27.
This study aims to further elucidate the role of adrenergic transmission in erection and to highlight whether adrenergic transmission in the penis modulates sildenafil's action.
Measurement of intracavernosal pressure in the anesthetized rat model.
Guanethidine (3 and 6 mg/kg) potentiated intracavernosal pressure/mean arterial pressure (ICP/MAP) rises in response to cavernous nerve stimulation by 4.375 ± 0.425 and 18.375 ± 1.085% respectively. Propranolol did the opposite. In presence of guanethidine, sildenafil (0.01, 0.1 and 1 mg/kg) potentiated ICP/MAP responses by 81.571 ± 4.918%, 147.83 ± 10.864% and 279.285 ± 23.053% at 1 Hz compared to 22.277 ± 2.139%, 123.571 ± 8.443% and 186.25 ± 13.542% respectively in the absence of guanethidine. Propranolol inhibited the effect sildenafil at all frequencies of stimulation. Verapamil exhibited a pro-erectile action and potentiated the effect of sildenafil (0.01, 0.1 and 1 mg/kg) on erectile responses corresponding to 85.25 ± 6.716%, 146 ± 11.288% and 221.571 ± 19.032% respectively compared to 26.011 ± 1.911%, 87.142 ± 8.73% and 182.2 ± 16.921% in its absence.
This study provides functional evidence that inhibition of sympathetic tone peripherally results in enhancement of erectile function. β-adrenergic receptors seem to play an important role in erection. The combination of sildenafil and guanethidine or verapamil could have a potential advantage on erectile function but propranolol may mask the effect of sildenafil on erectile function.
本研究旨在进一步阐明肾上腺素能传递在勃起中的作用,并强调阴茎中的肾上腺素能传递是否调节西地那非的作用。
在麻醉大鼠模型中测量海绵体内压。
胍乙啶(3 和 6 mg/kg)分别使对海绵体神经刺激的海绵体内压/平均动脉压(ICP/MAP)升高 4.375 ± 0.425%和 18.375 ± 1.085%。普萘洛尔则相反。在胍乙啶存在的情况下,西地那非(0.01、0.1 和 1 mg/kg)分别使 1 Hz 时的 ICP/MAP 反应增强 81.571 ± 4.918%、147.83 ± 10.864%和 279.285 ± 23.053%,而在没有胍乙啶的情况下,分别增强 22.277 ± 2.139%、123.571 ± 8.443%和 186.25 ± 13.542%。普萘洛尔抑制了西地那非在所有刺激频率下的作用。维拉帕米表现出促勃起作用,并增强了西地那非(0.01、0.1 和 1 mg/kg)对勃起反应的作用,相应地增强了 85.25 ± 6.716%、146 ± 11.288%和 221.571 ± 19.032%,而在没有维拉帕米的情况下,增强了 26.011 ± 1.911%、87.142 ± 8.73%和 182.2 ± 16.921%。
本研究提供了功能证据,表明外周抑制交感神经张力会增强勃起功能。β-肾上腺素能受体在勃起中似乎起着重要作用。西地那非与胍乙啶或维拉帕米联合使用可能对勃起功能有潜在优势,但普萘洛尔可能会掩盖西地那非对勃起功能的作用。